8 results
·
86ms
·
Sources: EU EUDAMED, US FDA
HOMER MAMMOLOK
FDA Adverse Event
Other
·NORTH AMERICAN INSTRUMENT CORP.·Product code MIJ·May 17, 1994
HOMER MAMMOLOK
FDA Adverse Event
Injury
·NORTH AMERICAN INSTRUMENT CORP.·Product code MIJ·May 17, 1994
HOMER MAMMOLOK
FDA Adverse Event
Malfunction
·NORTH AMERICAN INSTRUMENT CORP.·Product code MIJ·May 17, 1994
mdi Europa GmbH
Authorized representative
🇩🇪 Germany·132 Manufacturers·4741 Devices
Obelis s.a.
Authorized representative
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MedPath GmbH
Authorized representative
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Medical Technology Promedt Consulting GmbH
Authorized representative
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Advena Limited
Authorized representative
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